Clinical Research Associate

3 days ago

Australia Novotech Full time $104,000 - $130,878 per year

The Clinical Research Associate (CRAII - CRAIII), is primarily responsible for ensuring the rights and wellbeing of trial participants are protected and the reported trial data are accurate, complete, and verifiable from the source documents. The CRA is the primary contact between the Investigational Sites, Novotech and Sponsor. Key responsibility of a CRA is as a site relationship manager ensuring that clinical trials are conducted in accordance with ICH GCP guidelines, local and global regulatory requirements, and Novotech/Client SOPs.

We offer hybrid working arrangements and full flexibility in working hours to ensure our staff achieve the work-life balance often missing in this role.

Minimum Qualifications & Experience

Graduate in a clinical or life sciences-related field. Relevant experience/qualifications in allied professions may also be considered. Must have good time management skills, attention to detail, be able to work well in a team, and be computer literate. For our current opportunities we require experience of working in the research, pharmaceutical industry or a related field per job level as follows:

  • CRA II: minimum of 6 months of CRA independent monitoring experience
  • CRA III: 2+ years of CRA independent monitoring experience

You must have full unrestricted working rights in Australia to be considered for this role . We unfortunately cannot provide sponsorship for this role.

Responsibilities:

  • CRAs primary responsibility is to build relationships with Principal Investigators, study coordinators, pharmacists, and all relevant site trial personnel to ensure the efficient, expedited and smooth management of clinical trials.
  • Foster internal and external customer relationships to ensure focus on efficient, timely and productive project delivery as per study requirements and timelines.
  • collaboration with the In-house Clinical Research Associate (IHCRA) and Regulatory Start Up Associate (RSA), prepare site essential documents, and support the ethics and regulatory submission and approval processes as needed.
  • In collaboration with Regulatory Start-up (RSU) Team, understand the requirements of applicable local and international regulatory requirements as relevant to specific clinical trials.
  • Ensure recruitment of participants as per the site target. Drive site recruitment and engagement initiatives and prepare site-specific recruitment plan(s) and update as required.
    Monitoring of investigational sites as per ICH GCP This includes all monitoring visit types across all phases of a clinical trial including Site Selection, Site Initiation, Site Monitoring and Site Close Out, unblinded pharmacy visits, and co-monitoring visits. Visits can be conducted either onsite or remote as per CMP.

Novotech is proud to offer a great workplace. We are committed to being an employer of choice for gender equality and providing an inclusive work environment where everyone is treated fairly and with respect.

Our team members are passionate about what we do, but we understand work is only one of the things that is important to them. We support our team members with flexible working options, paid parental leave for both parents, flexible leave entitlements, wellness programs and ongoing development programs.

We are looking for people who are passionate about working clinical research and biotech, including people who identify as LGBTIQ+, have a disability or have caring responsibilities.

We are a Circle Back Initiative Employer and commit to respond to every application. We look forward to contacting you regarding your application.

  • Clinical Research Associate

    2 days ago

    Australia Icon Strategic Solutions Full time

    Overview(Senior) Clinical Research Associate FSP Global Pharma – Location: home-based in Sydney, Brisbane or Melbourne.As a Senior Clinical Research Associate, you will be joining the world's largest & most comprehensive clinical research organisation, powered by healthcare intelligence. You will have an opportunity to work in a solid partnership and an...

  • Clinical Research Assistant

    2 days ago

    Australia Qimr Berghofer Medical Research Institute Full time

    Part-time opportunity- Gain hands-on experience in clinical trial coordination- Attractive salary packaging & superannuation options**About QIMR Berghofer**:QIMR Berghofer is a world-leading translational medical research institute focused on improving health by developing new diagnostics, better treatments and prevention strategies, specifically in the...

  • Qa Associate

    2 days ago

    Australia Avance Clinical Full time

    **This is a rare opportunity to join our high performing QA team. If you are currently working for a CRO or Pharma organisation in GCP Quality Assurance, then we'd love to hear from you.*****Adelaide - office based*****Who are we?**We're Avance Clinical an Australian based Contract Research Organisation. We offer specialised services supporting drug...

  • CRA Opportunities

    5 days ago

    Australia Avance Clinical Full time $90,000 - $120,000 per year

    Australian based CRA positions - location flexible - work from home Due to our continued expansion, we're looking for experienced Clinical Research Associates (CRA's) to join our amazing, Australian based, Clinical Operations team where we have the following opportunities available. CRA II - 18 Months Experience As a CRACRA III - 2 years experience as a...

  • Clinical Research Orthoptist

    5 days ago

    Australia Aboriginal Health Full time $60,000 - $90,000 per year

    Reference Number: 1193Job Type: Part TimeDepartment: Research SalariesDescription:About the RolePart time fixed term (12 months)The Research Orthoptist/Research Assistant plays a key role in delivering high-quality research support to the Vitreoretinal Unit at the Royal Victorian Eye and Ear Hospital. Working as part of a team of ophthalmic clinicians and...

  • Cta I

    3 days ago

    Australia Avance Clinical Full time

    **Full time, permanent, office based position at our Head Office in Firle, South Australia.****Who are we?**We're Avance Clinical a Contract Research Organisation. We offer specialised services supporting drug development for the pharmaceutical and biotechnology industry. We have a rich history in this area with our founding roots dating back to the 1980's....

  • Research Associate

    2 days ago

    Australia Federal Reserve Bank Of Richmond Full time

    Research Associate 2026 - Washington, DCJoin to apply for theResearch Associate 2026 - Washington, DCrole atFederal Reserve Bank of RichmondCompanyFederal Reserve Bank of RichmondWhen you join the Federal Reserve—the nation's central bank—you'll play a key role, collaborating with leading tech professionals to strengthen and protect our economic,...

  • Senior Research Associate

    1 week ago

    Australia Unsw Full time

    Senior Research Associate - Pure Mathematics UNSW Canberra, Australian Capital Territory, AustraliaJoin or sign in to find your next job Join to apply for the Senior Research Associate - Pure Mathematics role at UNSWSenior Research Associate - Pure Mathematics UNSW Canberra, Australian Capital Territory, Australia2 days ago Be among the first 25...

  • Research Associate in Palliative Care

    2 days ago

    Australia beBeePalliative Full time $127,436 - $132,533

    Research Associate in Palliative CareHammondCare is seeking a highly motivated Research Associate to join its palliative care research team. The successful candidate will have the opportunity to contribute to the development and implementation of HammondCare's palliative care research strategy.Provide academic research support to senior palliative care...

  • Clinical Research Administrator

    2 days ago

    Australia beBeeClinical Full time $42,185 - $46,626

    Role OverviewThe Clinical Trials Coordinator will be a vital member of our clinical trials team, responsible for the planning, implementation, and coordination of clinical trials within the unit.Key ResponsibilitiesAssist with ethical and medico-legal requirements of setting up and undertaking drug/device clinical trials as part of multi-national, national,...